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	1.	The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual: Broadening the clinical phenotype. [electronic resource] by Bertola, Débora Yamamoto, Guilherme Buscarilli, Michelle Jorge, Alexander Passos-Bueno, Maria Rita Kim, Chong Producer: 20171019 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp. [electronic resource] by Bertola, Débora Buscarilli, Michelle Stabley, Deborah L Baker, Laura Doyle, Daniel Bartholomew, Dennis W Sol-Church, Katia Gripp, Karen W Producer: 20170508 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Further evidence of the importance of RIT1 in Noonan syndrome. [electronic resource] by Bertola, Débora R Yamamoto, Guilherme L Almeida, Tatiana F Buscarilli, Michelle Jorge, Alexander A L Malaquias, Alexsandra C Kim, Chong A Takahashi, Vanessa N V Passos-Bueno, Maria Rita Pereira, Alexandre C Producer: 20160516 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. [electronic resource] by Yamamoto, Guilherme Lopes Aguena, Meire Gos, Monika Hung, Christina Pilch, Jacek Fahiminiya, Somayyeh Abramowicz, Anna Cristian, Ingrid Buscarilli, Michelle Naslavsky, Michel Satya Malaquias, Alexsandra C Zatz, Mayana Bodamer, Olaf Majewski, Jacek Jorge, Alexander A L Pereira, Alexandre C Kim, Chong Ae Passos-Bueno, Maria Rita Bertola, Débora Romeo Producer: 20160224 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genotype and phenotype spectrum of NRAS germline variants. [electronic resource] by Altmüller, Franziska Lissewski, Christina Bertola, Debora Flex, Elisabetta Stark, Zornitza Spranger, Stephanie Baynam, Gareth Buscarilli, Michelle Dyack, Sarah Gillis, Jane Yntema, Helger G Pantaleoni, Francesca van Loon, Rosa LE MacKay, Sara Mina, Kym Schanze, Ina Tan, Tiong Yang Walsh, Maie White, Susan M Niewisch, Marena R García-Miñaúr, Sixto Plaza, Diego Ahmadian, Mohammad Reza Cavé, Hélène Tartaglia, Marco Zenker, Martin Producer: 20170928 In: European journal of human genetics : EJHG vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)